SCRA

A leading Biotech are seeking to appoint a Senior Clinical Research Associate to monitor activities associated with Clinical Trials, in accordance with Company SOPs and regulatory guidelines.

This position is an office based position in Surrey, with approximately 30% of this time being spent outside of the office.

Main Responsibilities (to include but not be limited to):

+ Site monitoring, as and when is needed

+ Responsible for the monitoring of Clinical Studies to ensure they are in accordance with Protocol, Company SOPs, and GCP guidelines

+ Responsible for reviewing data and providing feedback to Vendor site monitors

+ Assists in the identification of Investigators, and the preparation of Investigator meetings

+ Oversees Vendor CRA monitoring activities

+ Contributes towards the Operational effectiveness of the Department, alongside Senior Management

Skills/Experience:

+ Degree educated in Life Science/Science degree

+ At least five years experience within Clinical Research

+ Minimum 3 years experience as a CRA

+ Experience of working on international Phase II/III studies is highly desirable

+ Fluency in an additional European language would be advantageous.

This is a fantastic opportunity for the successful candidate to secure a permanent position within a reputable organisation.

To find out more about Real Staffing please visit www.realstaffing.com